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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289821Generated: October 29, 2026

Triethylamine → Diisopropyl Ether

https://huagongshe.com/reaction/2289821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-Dichloroisoquinoline-7-sulfonyl chlorideHCID 16658294—
ReactantNalpha-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-Nepsilon-tert-butyloxycarbonyl-L-lysine tert-butyl esterHCID 21969824—
Reactant7750-45-0HCID 51358437—
SolventDichloromethaneHCID 6344—
ProductDiisopropyl EtherHCID 7914—
ProductNalpha-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-Nepsilon-tert-butyloxycarbonyl-L-lysine tert-butyl esterHCID 21969824—

Reaction Steps

Nα-[(1,4-Dichloro-7-isoquinolinyl)sulphonyl]-Nε-tert-butyloxycarbonyl-L-lysine tert-butyl ester ##STR190## A solution of 1,4-dichloro-7-isoquinolinylsulphonyl chloride (250 mg, 0.84 mmol), Ne-tert-butyloxycarbonyl-L-lysine tert-butyl ester hydrochloride (286 mg, 0.84 mmol) and triethylamine (235 μl, 1.69 mmol) in CH2Cl2 (25 ml) was stirred at 23° C. for 3h. The reaction mixture was washed with water (2×20 ml), dried (MgSO4) and concentrated in vacuo to a residue which upon trituration with hexane and then i-Pr2O gave Nα-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-Nε-tert-butyloxycarbonyl-L-lysine tert-butyl ester as a white powder (270 mg, 0.48 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-f0bce4b963bb48e8bdb4bbce261066aa
Source noteuspto-grants-2000_07